Who have Taenia solium with Zithromax - from FDA reports


There is no Taenia solium reported by people who take Zithromax yet. This review analyzes which people have Taenia solium with Zithromax. It is created by eHealthMe based on reports from FDA, and is updated regularly.

How to use this study: bring a copy to your health teams to ensure drug risks and benefits are fully discussed and understood.


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On Feb, 21, 2019

No report is found.

Do you have Taenia solium while taking Zithromax?


You are not alone:




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Zithromax

Zithromax has active ingredients of azithromycin. It is often used in sinusitis. (latest outcomes from Zithromax 28,547 users)

Taenia Solium

Taenia solium has been reported by people with breast cancer metastatic, epilepsy, osteopenia, osteoporosis, convulsion (latest reports from 79 Taenia solium patients).


Drugs that are associated with Taenia solium
Taenia solium
Could your condition cause Taenia solium
Taenia solium
Zithromax side effects

Browse by gender and age

Female: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

Male: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+


Browse all side effects of Zithromax
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Compare Zithromax to similar drugs:


What would happen?

Predict new side effects and undetected conditions when you take Zithromax and have Taenia solium




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NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.

WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.

DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.

You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.

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